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Silphiperfol-5-en-3-ol B

PubChem CID: 91747332

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Compound Synonyms Silphiperfol-5-en-3-ol B, KACKPLUHPMMFBK-BZUNZJMGSA-N, Q67880097
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 20.2
Hydrogen Bond Donor Count 1.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CC2CCC3CCCC23C1
Np Classifier Class Silphiperfolane sesquiterpenoids
Deep Smiles C[C@H]CC[C@@][C@@H]5C[C@H][C@]5C)C=CC8C))C))))O
Heavy Atom Count 16.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CC2CCC3CCCC23C1
Classyfire Subclass Sesquiterpenoids
Isotope Atom Count 0.0
Molecular Complexity 358.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name (1S,5R,6R,8R,9S)-2,3,5,9-tetramethyltricyclo[6.3.0.01,5]undec-3-en-6-ol
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 3.5
Gsk 4 400 Rule True
Molecular Formula C15H24O
Scaffold Graph Node Bond Level C1=CC2CCC3CCCC23C1
Inchi Key KACKPLUHPMMFBK-BZUNZJMGSA-N
Silicos It Class Soluble
Rotatable Bond Count 0.0
Synonyms silphiperfol-5-en-3-ol b
Esol Class Soluble
Functional Groups CC(C)=CC, CO
Compound Name Silphiperfol-5-en-3-ol B
Exact Mass 220.183
Formal Charge 0.0
Monoisotopic Mass 220.183
Hydrogen Bond Acceptor Count 1.0
Molecular Weight 220.35
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 6.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C15H24O/c1-9-5-6-15-11(3)10(2)8-14(15,4)13(16)7-12(9)15/h8-9,11-13,16H,5-7H2,1-4H3/t9-,11?,12+,13+,14-,15+/m0/s1
Smiles C[C@H]1CC[C@@]23[C@@H]1C[C@H]([C@@]2(C=C(C3C)C)C)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Sesquiterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Artemisia Laciniata (Plant) Rel Props:Reference:https://doi.org/10.1002/(sici)1099-1026(199709/10)12:5<315::aid-ffj662>3.0.co;2-q